Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

95 matching diseasesClear search ×

KBG syndrome

Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome · ANKRD11-related disorder

ORPHA:2332

Laryngeal abductor paralysis-intellectual disability syndrome

Plott syndrome

ORPHA:2375

Macrocephaly-intellectual disability-autism syndrome

ORPHA:210548

Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome

Sohval-Soffer syndrome

ORPHA:2234

MAN1B1-CDG

Congenital disorder of glycosylation type 2 due to MAN1B1 deficiency · Congenital disorder of glycosylation type II due to MAN1B1 deficiency

ORPHA:397941

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

Mesomelic dysplasia-digital anomalies-intellectual disability syndrome

ORPHA:632603

Microcephaly-digital anomalies-intellectual disability syndrome

Kelly-Kirson-Wyatt syndrome

ORPHA:137653

Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome

Woods-Crouchman-Huson syndrome

ORPHA:137658

Mirhosseini-Holmes-Walton syndrome

Pigmentary retinopathy-intellectual disability syndrome

ORPHA:3084

Mowat-Wilson syndrome

Hirschsprung disease-intellectual disability syndrome

ORPHA:2152

Multiple congenital anomalies/dysmorphic syndrome without intellectual disability

MCA without intellectual disability · Multiple congenital anomalies without intellectual disability with or without dysmorphism

ORPHA:102285

Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

MCA/MR · Multiple congenital anomalies-intellectual disability with or without dysmorphism

ORPHA:102283

OBSOLETE: Atrichia-intellectual disability and growth delay syndrome

ORPHA:1211

OBSOLETE: Cataract-intellectual disability-anal atresia-urinary defects syndrome

OBSOLETE: Karandikar-Maria-Kamble syndrome

ORPHA:1381

OBSOLETE: Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

OBSOLETE: Genetic MCA/variable MR · OBSOLETE: Genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome

ORPHA:330197

OBSOLETE: Intellectual disability-unusual facies syndrome

OBSOLETE: Morillo Cucci-Passarge syndrome

ORPHA:3043

OBSOLETE: Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

OBSOLETE: MCA/variable MR · OBSOLETE: Multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome

ORPHA:102284

OBSOLETE: Trichodermal syndrome-intellectual disability syndrome

OBSOLETE: Katsantoni-Papadakou Lagoyanni syndrome

ORPHA:3360

Optic atrophy-intellectual disability syndrome

BBSOAS · Bosch-Boonstra-Schaaf optic atrophy syndrome

ORPHA:401777

Osteopenia-intellectual disability-sparse hair syndrome

Kaler-Garrity-Stern syndrome

ORPHA:2324

Pachygyria-intellectual disability-epilepsy syndrome

Kuzniecky syndrome

ORPHA:2798

Pinsky-Di George-Harley syndrome

Microphthalmia-intellectual disability syndrome

ORPHA:2895

Primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome

ORPHA:620363

Proximal Xq28 duplication syndrome

MECP2 duplication syndrome · X-linked intellectual disability syndrome, Lubs type

ORPHA:1762

Pseudoprogeria syndrome

Hal-Berg-Rudolph syndrome · Absent eyebrows and eyelashes-intellectual disability syndrome

ORPHA:2985

Pterygium colli-intellectual disability-digital anomalies syndrome

Khalifa-Graham syndrome

ORPHA:2988

Ramos-Arroyo syndrome

Corneal anesthesia-hearing loss-intellectual disability syndrome · Corneal anesthesia-deafness-intellectual disability syndrome

ORPHA:1051

Rare genetic syndromic intellectual disability

ORPHA:183763

Rare non-syndromic intellectual disability

Rare NSID

ORPHA:101685

Rare syndromic intellectual disability

ORPHA:102369

Rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome

ORPHA:611314

Richards-Rundle syndrome

Ketoaciduria-intellectual disability-ataxia-deafness syndrome · Ketoaciduria-intellectual disability-ataxia-hearing loss syndrome

ORPHA:1399

Richieri Costa-da Silva syndrome

Myotonia-intellectual disability-skeletal anomalies syndrome

ORPHA:3101

Seizures-intellectual disability due to hydroxylysinuria syndrome

ORPHA:79156

SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome

ORPHA:597743

Short stature-intellectual disability-eye anomalies-cleft lip/palate syndrome

Richieri Costa-Guion Almeida syndrome

ORPHA:2649

Spastic paraplegia-glaucoma-intellectual disability syndrome

ORPHA:2818

Tall stature-intellectual disability-renal anomalies syndrome

Thauvin-Robinet-Faivre syndrome

ORPHA:500095

Trichomegaly-retina pigmentary degeneration-dwarfism syndrome

Oliver-McFarlane syndrome · Long eyelashes-intellectual disability syndrome

ORPHA:3363

Ulna hypoplasia-intellectual disability syndrome

ORPHA:2249

Urban-Rogers-Meyer syndrome

Intellectual disability-short stature-hand contractures-genital anomalies syndrome · Prader-Willi habitus-osteopenia-camptodactyly syndrome

ORPHA:3409

Wilson-Turner syndrome

WTS · X-linked intellectual disability-gynecomastia-obesity syndrome

ORPHA:3459

Witteveen-Kolk syndrome

SIN3A-related intellectual disability syndrome · WITKOS

ORPHA:500163

X-linked alpha-thalassemia-intellectual disability syndrome

ATR-X syndrome

ORPHA:847

X-linked intellectual disability-ataxia-apraxia syndrome

ORPHA:85338

X-linked intellectual disability-epilepsy syndrome

ORPHA:2076